Dyslipidemia links obesity to early cerebral neurochemical alterations

Obesity (Silver Spring). 2013 Oct;21(10):2007-13. doi: 10.1002/oby.20332. Epub 2013 May 25.

Abstract

Objective: To examine the role of hypertension, hyperglycemia, and dyslipidemia in potentially accounting for obesity-related brain vulnerability in the form of altered cerebral neurochemistry.

Design and methods: Sixty-four adults, ages 40-60 years, underwent a health screen and proton magnetic resonance spectroscopy ((1) H MRS) of occipitoparietal gray matter to measure N-acetyl aspartate (NAA), choline (Cho), myo-inositol (mI), and glutamate (Glu) relative to creatine (Cr). The causal steps approach and nonparametric bootstrapping were utilized to assess if fasting glucose, mean arterial pressure or peripheral lipid/lipoprotein levels mediate the relationship between body mass index (BMI) and cerebral neurochemistry.

Results: Higher BMI was significantly related to higher mI/Cr, independent of age and sex. BMI was also significantly related to two of the proposed mediators, triglyceride, and HDL-cholesterol, which were also independently related to increased mI/Cr. Finally, the relationship between BMI and mI/Cr was significantly attenuated after inclusion of triglyceride and HDL-cholesterol into the model, one at a time, indicating statistical mediation.

Conclusions: Higher triglyceride and lower HDL levels statistically account for the association between BMI and myo-inositol, pointing toward a potentially critical role for dyslipidemia in the development of cerebral neurochemical alterations in obesity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / metabolism
  • Blood Glucose
  • Blood Pressure
  • Body Mass Index
  • Brain / physiopathology
  • Brain Diseases / etiology
  • Brain Diseases / physiopathology*
  • Cholesterol, HDL / blood
  • Choline / metabolism
  • Creatine / metabolism
  • Dyslipidemias / complications
  • Dyslipidemias / physiopathology*
  • Female
  • Glutamic Acid / metabolism
  • Humans
  • Inositol / metabolism
  • Linear Models
  • Magnetic Resonance Spectroscopy
  • Male
  • Middle Aged
  • Neurochemistry
  • Obesity / complications
  • Obesity / physiopathology*
  • Triglycerides / blood

Substances

  • Blood Glucose
  • Cholesterol, HDL
  • Triglycerides
  • Aspartic Acid
  • Glutamic Acid
  • Inositol
  • N-acetylaspartate
  • Creatine
  • Choline